Sulfotransferase 1A3/4 copy number variation is associated with neurodegenerative disease
Article in The Pharmacogenomics Journal (April 2017)
The most recent citing publications are shown below. View all 4 publications that cite this research output on Dimensions.
Characterization of 14 novel deletions underlying Rubinstein–Taybi syndrome: an update of the CREBBP deletion repertoire
Article in Human Genetics (March 2015)
Patent ductus arteriousus device closure in an infant with rubinstein-taybi syndrome.
Article in Iranian Journal of Pediatrics (December 2013)